Dietary salicylates affect calcium and magnesium status in preeclampsia model rats induced by NG-nitro-L-arginine-methyl ester (L-NAME).

IF 3.3
Rafsan Syabani Cholik, Katarzyna Skrypnik, Marta Karaźniewicz-Łada, Agnieszka Waśkiewicz, Joanna Suliburska
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Abstract

Preeclampsia (PE) represents a complex hypertensive disorder of pregnancy which combines blood pressure elevation with organ dysfunction through mineral metabolism disturbances. The current guidelines recommend low-dose aspirin for PE prevention yet the impact of dietary salicylates on mineral status remains an open question. This research investigated how dietary salicylates and aspirin affect calcium and magnesium homeostasis in rats with NG-nitro-L-arginine-methyl ester (L-NAME)-induced preeclampsia. The research involved pregnant Sprague Dawley rats who received six different treatment groups: CH (healthy controls) and PE (preeclamptic controls) alongside four intervention groups that combined L-NAME with low or high dietary salicylates (LSP, HSP) or aspirin (LAP, HAP). The preeclampsia model used L-NAME (0.5 mg/mL) throughout gestational days 6-19. The flame atomic absorption spectrometry method measured calcium and magnesium levels in tissues and serum samples. The high-performance liquid chromatography (HPLC) and the ultra-high performance liquid chromatography-tandem mass spectrometry system (UHPLC-MS/MS) analyzed salicylic acid concentrations. The administration of L-NAME resulted in elevated blood pressure together with elevated calcium levels in placental and renal tissues. The tissue magnesium (Mg) levels increased in heart and brain tissues when animals consumed salicylates or aspirin without any effect on blood pressure. The combination of high salicylate intake resulted in reduced calcium (Ca) levels in femoral tissues and decreased albumin excretion in urine. The Ca:Mg molar ratio changed significantly in kidney tissue as well as placenta tissue and pancreas tissue. The preeclampsia condition caused by L-NAME disrupts the normal distribution of calcium and magnesium throughout maternal and fetal body tissues.

饮食中水杨酸对ng -硝基- l -精氨酸甲酯(L-NAME)诱导的子痫前期模型大鼠钙镁状态的影响。
先兆子痫(PE)是一种复杂的妊娠高血压疾病,通过矿物质代谢紊乱结合血压升高和器官功能障碍。目前的指南推荐低剂量阿司匹林用于PE预防,但饮食中的水杨酸对矿物质状态的影响仍然是一个悬而未决的问题。本研究探讨了饮食中水杨酸盐和阿司匹林对ng -硝基- l -精氨酸甲酯(L-NAME)诱导的子痫前期大鼠钙镁稳态的影响。这项研究涉及怀孕的斯普莱格·道利大鼠,这些大鼠接受了6个不同的治疗组:CH(健康对照组)和PE(子痫前期对照组),以及4个将L-NAME与低或高饮食水杨酸(LSP, HSP)或阿司匹林(LAP, HAP)联合使用的干预组。子痫前期模型在妊娠6-19天使用L-NAME(0.5 mg/mL)。火焰原子吸收光谱法测定组织和血清样品中的钙、镁含量。采用高效液相色谱(HPLC)和超高效液相色谱-串联质谱系统(UHPLC-MS/MS)分析水杨酸浓度。L-NAME的使用导致血压升高,胎盘和肾组织中钙水平升高。当动物食用水杨酸盐或阿司匹林时,心脏和脑组织中的组织镁(Mg)水平升高,而对血压没有任何影响。高水杨酸摄入的组合导致股骨组织中钙(Ca)水平降低和尿中白蛋白排泄减少。肾组织、胎盘组织和胰腺组织Ca:Mg摩尔比发生显著变化。L-NAME引起的子痫前期破坏了钙和镁在母体和胎儿身体组织中的正常分布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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